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酵母质粒的染色体整合与缺失分析

Analysis of chromosomal integration and deletions of yeast plasmids.

作者信息

Cameron J R, Philippsen P, Davis R W

出版信息

Nucleic Acids Res. 1977;4(5):1429-48. doi: 10.1093/nar/4.5.1429.

Abstract

Plasmid DNAs from six strains of Saccharomyces cerevisiae were compared. Three different plasmids were found, designated Scp 1, Scp 2 and Scp 3, with monomer lengths of 6.19, 6.06 and 5.97 kilobases as referenced to sequenced phiX174 DNA. DNA from each of the plasmids was inserted into a lambda vector DNA. Hybrid phage containing inserted DNA of the desired size were enriched by genetic selection and their DNAs analysed by rapid techniques. All three plasmids share the same organization, two unique sequences separated by two inverted repeats, and share basically the same DNA sequences. Scp 2 and Scp 3 differ from Scp 1 by missing a unique HpaI site and by having small overlapping deletions in the same region. The HpaI site in Scp 1 is, therefore, in a nonessential region and suitable for insertion of foreign DNA in the potential use of the yeast plasmid as a vector. Hybridization of labelled cloned plasmid DNA to restriction fragments of linear yeast DNA separated on agarose gels showed that the plasmid DNA was not stably integrated into the yeast chromosomal DNA.

摘要

对六株酿酒酵母的质粒DNA进行了比较。发现了三种不同的质粒,分别命名为Scp 1、Scp 2和Scp 3,以测序的phiX174 DNA为参照,其单体长度分别为6.19、6.06和5.97千碱基。将每个质粒的DNA插入λ载体DNA中。通过遗传筛选富集含有所需大小插入DNA的杂交噬菌体,并通过快速技术分析其DNA。所有三种质粒具有相同的结构,即由两个反向重复序列隔开的两个独特序列,并且基本具有相同的DNA序列。Scp 2和Scp 3与Scp 1的不同之处在于缺少一个独特的HpaI位点,并且在同一区域有小的重叠缺失。因此,Scp 1中的HpaI位点位于非必需区域,在将酵母质粒用作载体的潜在用途中适合插入外源DNA。用标记的克隆质粒DNA与在琼脂糖凝胶上分离的线性酵母DNA的限制性片段杂交,结果表明质粒DNA未稳定整合到酵母染色体DNA中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6a1/343766/4ad0ddfe2b41/nar00478-0276-a.jpg

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